24 Alisch Alisch RS RS Wang Wang T T Chopra Chopra P P et al et al Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus BMC Med Genet BMC Med Genet 2013 2013 10.1186/1471-2350-14-18 10.1186/1471-2350-14-18. The gene discussed is FMR1; the disease is fragile X syndrome.